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奎奴普丁/达福普汀对耐万古霉素屎肠球菌菌血症结局的影响:与对照队列的比较

Effect of quinupristin/dalfopristin on the outcome of vancomycin-resistant Enterococcus faecium bacteraemia: comparison with a control cohort.

作者信息

Linden P K, Pasculle A W, McDevitt D, Kramer D J

机构信息

Department of Medicine, University of Pittsburgh Medical Center, PA, USA.

出版信息

J Antimicrob Chemother. 1997 May;39 Suppl A:145-51. doi: 10.1093/jac/39.suppl_1.145.

Abstract

Serious infection with vancomycin-resistant Enterococcus faecium (VREF) strains has no proven effective antimicrobial therapy. We compared the clinical and bacteriological outcomes of 20 patients with VREF bacteraemia treated with quinupristin/dalfopristin (RP 59500), an investigational streptogramin, with a historical cohort of 42 patients with VREF bacteraemia treated with other agents. Quinupristin/dalfopristin demonstrated in-vitro bacteriostatic activity against all 20 initial VREF blood isolates (MIC range 0.03-0.50 mg/L) by macrobroth dilution. The clinical characteristics of both groups were comparable for major outcome-dependent variables. There were five cases of recurrent VREF bacteraemia in the quinupristin/dalfopristin-treated cohort and 21 in the controls (P = 0.11); persistence of VREF at the primary site was found in six and 18 of the evaluable patients with follow-up cultures in these two cohorts (P = 0.06). In-hospital mortality was high in both groups: 65% in the quinupristin/dalfopristin group and 52% in the control group; however, VREF-associated mortality was significantly lower in the quinupristin/dalfopristin group (five and 17 respectively; P = 0.05). Follow-up susceptibility testing of five VREF isolates in the quinupristin/ dalfopristin group did not demonstrate resistance to quinupristin/dalfopristin. Quinupristin/ dalfopristin may be a useful agent for the therapy of serious VREF infection. Further clinical investigations are warranted to confirm or refute its clinical efficacy.

摘要

耐万古霉素粪肠球菌(VREF)菌株的严重感染尚无经证实有效的抗菌治疗方法。我们比较了20例接受喹奴普汀/达福普汀(RP 59500,一种试验性链阳菌素)治疗的VREF菌血症患者与42例接受其他药物治疗的VREF菌血症患者的历史队列的临床和细菌学结果。通过常量肉汤稀释法,喹奴普汀/达福普汀对所有20株初始VREF血液分离株均表现出体外抑菌活性(MIC范围为0.03 - 0.50 mg/L)。两组的主要结局相关变量的临床特征具有可比性。喹奴普汀/达福普汀治疗组有5例复发性VREF菌血症,对照组有21例(P = 0.11);在这两个队列中,可评估患者的随访培养中,原发部位VREF持续存在的情况分别为6例和18例(P = 0.06)。两组的住院死亡率都很高:喹奴普汀/达福普汀组为65%,对照组为52%;然而,喹奴普汀/达福普汀组与VREF相关的死亡率显著较低(分别为5例和17例;P = 0.05)。喹奴普汀/达福普汀组对5株VREF分离株的随访药敏试验未显示对喹奴普汀/达福普汀耐药。喹奴普汀/达福普汀可能是治疗严重VREF感染的一种有用药物。有必要进行进一步的临床研究以证实或反驳其临床疗效。

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